ANSH LABS Us AMH/ MIS Elisa - Indonesia BPOM Medical Device Registration
ANSH LABS Us AMH/ MIS Elisa is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220274. The device is manufactured by ANSH LABS LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTI MAKMUR MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANSH LABS LLC.Country of Origin
United States
Authorized Representative
PT. INTI MAKMUR MEDITAMAAR Address
JL. SULTAN ISKANDAR MUDA, GANDARIA 8 OFFICE TOWER LANTAI 16 UNIT F, KEBAYORAN LAMA JAKARTA SELATAN
Registration Date
Mar 09, 2022
Expiry Date
Dec 31, 2024
Product Type
Clinical Chemistry Test System
Human growth hormone test system (kit & cair)
Invitro Diagnostics
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